Annotation Detail

Information
Associated Genes
RBM20
Associated Variants
RBM20 p.Thr653Ile (p.T653I) ( ENST00000369519.4 )
RBM20 p.Thr653Ile (p.T653I) ( ENST00000369519.4 )
Associated Disease
not provided
Source Database
ClinVar
Description
NM_001134363.3(RBM20):c.1958C>T (p.Thr653Ile) AND not provided
ClinVar Allele ID
174874
ClinVar RefSeq Alternation Syntax
NM_001134363.3:c.1958C>T
Clinical Significance Description
Uncertain significance
Clinical Significance Last Update
2022-11-16
Clinical Significance Review Status
criteria provided, single submitter
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000766690
ClinVar Disease
not provided
Observed Origin Sample
germline
Drugs